Cytoskeletal elements are required for the formation and maturation of autophagic vacuoles

J Cell Physiol. 1992 Sep;152(3):458-66. doi: 10.1002/jcp.1041520304.

Abstract

We evaluated the role of cytoskeletal elements in the degradation of endogenous proteins via autophagy using biochemical and morphological techniques. In the absence of exogenous amino acids, degradation of endogenous proteins was enhanced in cultured normal rat kidney cells. This enhanced degradative state was accompanied by a 4-fold increase in the occurrence of autophagic vacuoles. In the presence of drugs that induce the depolymerization of microfilaments (cytochalasins B and D) or microtubules (nocodazole), protein degradation was not enhanced in nutrient-deprived cells. Although these drugs had similar inhibitory effects on the protein degradation, their effect on autophagy differed. Cytochalasins B and D interfered with the formation of the autophagosome. In cells treated with these drugs, the fractional volume represented by autophagic vacuoles was not substantially increased despite nutrient depletion. On the contrary, nocodazole appeared to have no effect on the formation of autophagosomes. Instead, this drug suppressed the delivery of hydrolytic enzymes, thereby resulting in an accumulation of acidic autophagic vacuoles containing undegraded cellular components.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / physiology
  • Animals
  • Autophagy / drug effects*
  • Cell Line
  • Colchicine / pharmacology
  • Cytochalasin B / pharmacology*
  • Cytochalasin D / pharmacology*
  • Microtubules / drug effects
  • Microtubules / physiology
  • Nocodazole / pharmacology*
  • Proteins / metabolism
  • Rats
  • Vacuoles / drug effects*
  • Vacuoles / ultrastructure

Substances

  • Proteins
  • Cytochalasin D
  • Cytochalasin B
  • Nocodazole
  • Colchicine